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NEW JERSEY CHAPTER

  • 2006 - 2011

     

past events



  • 2011- program
    • Bayesian Goldilocks Designs: Getting the Sample Size Just Right, Scott M. Berry
    • Adapting Traditional Adaptive Designs: New Methods and Procedures, Scott Evans
    • Efficient Two-Stage Adaptive Designs with Sample Size Adjustment, Qing Liu et. al
    • Bayesian and Frequentist Adaptive Designs in Clinical Trials, Gene Pennello
  • 2008
    • Case Studies of the Use of Meta-Analyses of Drug Safety Questions in the Regulatory Setting, Jesse A. Berlin
    • Role of Integrated Analysis in Regulatory Applications, H.M. James Hung
    • Integrated Dose-Exposure-Response Modeling and Use in Clinical Trial Simulation, Heinz Schmidli and Jerry R. Nedelman
    • Meta-analysis in randomized clinical trials with low event rates, Jonathan J. Shuster
  • 2007- program
    • Global Sensitivity Analysis for Randomized Trials with Competing Causes of Drop-out, Daniel O. Scharfstein
    • Non-inferiority Methodology in Drug Clinical Trial, H.M. James Hung
    • Sensitivity to MAR Assumption in Missing Data: Case Studies Using Model-Based Multiple Imputation, Jie Zhang and José Pinheiro
    • Parametric Modeling of Time-to-Event Data With Possibly Non-Proportional Hazards, Keaven Anderson

 

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